Safety Pharmacology

Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Manager to join our Clinical

.Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio

Department :Centralised Monitoring Unit (CMU): Bangalore Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a

Department – Centralised Monitoring Unit (CMU)- Bangalore Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a

Department :Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working

The job will involve: - Conducting regulated study protocol reviews, data and report audits for Toxicology, Safety Assessment and Pharmacology studies. -

Department: Regulatory Affairs Rare Blood Disorders Are you passionate about driving regulatory strategy and life cycle management of product portfolio

Department :Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working

Role: - Medical Writing Location: - Mumbai Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol,

Job Summary We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will

Department :Centralised Monitoring Unit (CMU): Bangalore Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a

Department :Centralised Monitoring Unit (CMU): Bangalore Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a